20 results
diagnosis dermatology rheumatology disease syphilis adultonset anemia antinxp2 antinxp2dm aplastic associated bacilliformis bartonella behcets cefepime cutaneous dermatomyositis dress erythematosus fever
Behcet's Syndrome - Treatment Ulcers: • Treatment: Topical steroids • Prevention: Colchicine • Azathioprine for refractory disease Arthritis:
Behcet's Syndrome ... lesions • Derm referral ... • Early ophtho referral ... case) • Surgery may ... #Treatment #management
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Macrophage Activation ... Syndrome (MAS) ... Petechial or purpuric rash ... Treatment: • Corticosteroids ... #Management #Hematology
Secondary Syphilis Rash Secondary syphilis is the most contagious of all the stages of this disease, and
with or without treatment ... , but without treatment ... appear as rough ... #Diagnosis #Clinical ... #Photo #Dermatology
Cefepime-induced red man syndrome in a 25-year-old male. #Cefepime #RedMan #Syndrome #Clinical #Photo #Dermatology #Rash
Cefepime-induced red man ... syndrome in a 25 ... Cefepime #RedMan #Syndrome ... #Clinical #Photo ... #Dermatology #Rash
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Still's Disease Clinical ... arthritis, Skin rash ... Complications: MAS ... Disease #diagnosis #management ... #treatment #rheumatology
Staphylococcus-associated GlomeruloNephritis - Diagnosis and Management Summary CLINICAL • Nephritic syndrome (Casts) • Marked proteinuria (may be
Diagnosis and Management ... Summary CLINICAL ... • Nephritic syndrome ... • Vasculitic rash ... deposits common TREATMENT
Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) Definition: • Severe adverse drug reaction, characterized by
extensive skin rash ... eruption that may ... disease: symptomatic treatment ... SinaiBmoreIMRes #DRESS #Syndrome ... #management
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
: Overwhelming clinical ... syndrome associated ... excessive macrophage activation ... Lymphohistiocytosis #diagnosis #management ... #treatment #hematology
Oroya Fever Hematologic disease caused by Bartonella bacilliformis Restricted to the Andes highlands of Peru & Ecuador B. bacilliformis:
Oroya Fever Hematologic ... jaundice ​• Neuro: AMS ... Clinical Presentation ... TREATMENT: ​• Acute ... Fever #diagnosis #management
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Constitutional Syndromes ... Aplastic Anemia Clinical ... aplastic anemia Treatment ... Anemia #oncology #hematology ... #diagnosis #management
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